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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5NO3
Molecular Weight 139.1088
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-NITROPHENOL

SMILES

OC1=CC=CC(=C1)[N+]([O-])=O

InChI

InChIKey=RTZZCYNQPHTPPL-UHFFFAOYSA-N
InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Catabolism of 3-Nitrophenol by Ralstonia eutropha JMP 134.
1997 Apr
Combined participation of hydroxylase active site residues and effector protein binding in a para to ortho modulation of toluene 4-monooxygenase regiospecificity.
2002 Mar 5
Relationship between strength of organic sorbate interactions in NOM and hydration effect on sorption.
2002 Nov 1
Mechanism of sorption of phenols from aqueous solutions onto surfactant-modified montmorillonite.
2002 Oct 15
Effect of three nitrophenols on carbon metabolism in Nostoc muscorum and Chlorella vulgaris.
2003 Jun
Simultaneous determination of phenol and mononitrophenol isomers using PLS regression and conventional and derivative spectrophotometry.
2005 Jan-Feb
Dynamic liquid-liquid-liquid microextraction with automated movement of the acceptor phase.
2005 Mar 15
Micellar enhanced ultrafiltration of phenolic derivatives from their mixtures.
2005 May 1
Probing actomyosin interactions with 2,4-dinitrophenol.
2005 May 15
Electropolymerized films formed from the amphiphilic decyl esters of D- and L-tyrosine compared to L-tyrosine using the electrochemical quartz crystal microbalance.
2005 May-Jun
Pairwise-substitution effects and intramolecular hydrogen bonds in nitrophenols and methylnitrophenols. Thermochemical measurements and ab initio calculations.
2007 Jul 19
Synthesis, characterization and catalytic application of silver nanoshell coated functionalized polystyrene beads.
2007 Jun
Analysis of the substituent effect on the reactivity modulation during self-protonation processes in 2-nitrophenols.
2007 Sep 20
Small-molecule aggregation inhibitors reduce excess amyloid in a trisomy 16 mouse cortical cell line.
2008
Pharmacodynamics of memantine: an update.
2008 Mar
(Z)-6-[(5-Chloro-2-hydroxy-anilino)-methyl-ene]-4-methoxy-cyclo-hexa-2,4-dienone 0.25-hydrate.
2009 Apr 25
3-Nitrophenol-4,4'-bipyridyl N,N'-dioxide (2/1): a DFT study and CSD analysis of DPNO molecular complexes.
2010 Aug
Kinetic studies and predictions on the hydrolysis and aminolysis of esters of 2-S-phosphorylacetates.
2010 Aug 16
Synthesis and insecticidal activity of novel carbamate derivatives as potential dual-binding site acetylcholinesterase inhibitors.
2010 Dec 22
Determination of partition coefficient and analysis of nitrophenols by three-phase liquid-phase microextraction coupled with capillary electrophoresis.
2010 Jul
A process optimization for bio-catalytic production of substituted catechols (3-nitrocatechol and 3-methylcatechol.
2010 Jun 30
Patents
Name Type Language
M-NITROPHENOL
MI  
Systematic Name English
M-NITROPHENOL [MI]
Common Name English
NSC-1551
Code English
1-HYDROXY-3-NITROBENZENE
Systematic Name English
NITROPHENOL, 3-
Systematic Name English
M-HYDROXYNITROBENZENE
Systematic Name English
3-NITROPHENOL
HSDB  
Systematic Name English
PHENOL, 3-NITRO-
Systematic Name English
PHENOL, M-NITRO-
Systematic Name English
3-HYDROXYNITROBENZENE
Systematic Name English
3-NITROPHENOL [HSDB]
Common Name English
Code System Code Type Description
FDA UNII
T6P4T52V9W
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
PUBCHEM
11137
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
CAS
554-84-7
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
MERCK INDEX
m7976
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY Merck Index
NSC
1551
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
HSDB
1337
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID2025765
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-073-5
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY
CHEBI
34346
Created by admin on Fri Dec 15 17:58:31 UTC 2023 , Edited by admin on Fri Dec 15 17:58:31 UTC 2023
PRIMARY